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Homocystinuria: A rare condition presenting as stroke and megaloblastic anemia
Parveen Bhardwaj1, Ravi Sharma, Minoo Sharma
1Department of Pediatrics, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Abstract:
Homocystinuria is an inborn error of amino acid metabolism in which homocystine accumulates in the blood and produces a slowly evolving clinical syndrome. We are presenting a case of a 4-year-old female child who presented to us with stroke and also had megaloblastic anemia. She was diagnosed as having homocystinuria type-1, and she responded to treatment.
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